


Product Usage Information
Important! This control antibody must be diluted to the same concentration (not dilution) as the specific antibody used in analysis. Higher background fluorescence may result if excessive amounts of isotype control are used. For protocol details, please reference the product page for the specific antibody used in analysis.


Specificity/Sensitivity




参考图片
Immunohistochemical analysis of paraffin-embedded human lung carcinoma using p53 (DO-7) Mouse mAb #48818 (left) compared to concentration matched Mouse (E7Q5L) mAb IgG2b Isotype Control (right).
Confocal immunofluorescent analysis of HCT 116 cells using β-Actin (8H10D10) Mouse mAb #3700 (left, green) compared to concentration matched Mouse (E7Q5L) mAb IgG2b Isotype Control (right, green). Red = Propidium Iodide (PI)/RNase Staining Solution #4087.
Flow cytometric analysis of HeLa cells using β-Actin (8H10D10) Mouse mAb #3700 (solid line) compared to concentration-matched Mouse (E7Q5L) mAb IgG2b Isotype Control (dashed line). Anti-mouse IgG (H+L), F(ab')2 Fragment (Alexa Fluor® 488 Conjugate) #4408 was used as a secondary antibody.
Chromatin immunoprecipitations were performed with cross-linked chromatin from 4 x 106 HCT116 cells treated with UV (1000 J/m2 followed by a 3 hour recovery) and either Mouse (E7Q5L) mAb IgG2b Isotype Control, Normal Rabbit IgG #2729, or p53 (DO-7) Mouse mAb #48818 using SimpleChIP® Plus Enzymatic Chromatin IP Kit (Magnetic Beads) #9005. The enriched DNA was quantified by real-time PCR using SimpleChIP® Human CDKN1A Promoter Primers #6449, SimpleChIP® Human MDM2 Intron 2 Primers #90678, and SimpleChIP® Human α Satellite Repeat Primers #4486. The amount of immunoprecipitated DNA in each sample is represented as signal relative to the total amount of input chromatin, which is equivalent to one.